39696-48-5

Basic information

• Product Name: 3H-1,2,4-Triazole-3-thione, 1,2-dihydro-2-methyl-5-phenyl-
• CAS NO: 39696-48-5
• Molecular Formula: C9H9N3S
• Molecular Weight: 191.257
• Mol File: 39696-48-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3H-1,2,4-Triazole-3-thione, 1,2-dihydro-2-methyl-5-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 3H-1,2,4-Triazole-3-thione, 1,2-dihydro-2-methyl-5-phenyl-(39696-48-5)
• EPA Substance Registry System: 3H-1,2,4-Triazole-3-thione, 1,2-dihydro-2-methyl-5-phenyl-(39696-48-5)

Safety Data

• Hazardous Substances Data: 39696-48-5(Hazardous Substances Data)

Upstream product

• 40398-30-9 N-(morpholinothiocarbonyl)benzamide 
• 60-34-4 methylhydrazine 
• 6938-68-7 2-methyl-thiosemicarbazide 
• 94-02-0 ethyl 3-oxo-3-phenylpropionate 
• 100706-03-4 3-(2-methyl-thiosemicarbazono)-3-phenyl-propionic acid ethyl ester 
• 76595-02-3 2-methyl-5-oxo-7-phenyl-3-thioxo-3,4,5,6-tetrahydro-2H-1,2,4-triazepine 
• 13281-42-0 1-Benzoyl-2-methyl-thiosemicarbazid 

Downstream Products

• 54034-38-7 1-methyl-3-phenyl-1,2,4-triazolin-5-one 
• 154106-10-2 5-Methanesulfinyl-1-methyl-3-phenyl-1H-[1,2,4]triazole 
• 129521-39-7 1-methyl-5-(methylsulfonyl)-3-phenyl-1H-1,2,4-triazole 
• 757920-22-2 (6R,7R)-7-{2-(2-Amino-thiazol-4-yl)-2-[(Z)-methoxyimino]-acetylamino}-3-(2-methyl-5-phenyl-2H-[1,2,4]triazol-3-ylsulfanylmethyl)-8-oxo-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid 
• 177713-78-9 (6R,7R)-7-Amino-3-(2-methyl-5-phenyl-2H-[1,2,4]triazol-3-ylsulfanylmethyl)-8-oxo-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid 
• 50369-47-6 1-methyl-5-(methylthio)-3-phenyl-1H-1,2,4-triazole 
• 39696-57-6 5-(2,4-dinitro-phenylsulfanyl)-1-methyl-3-phenyl-1H-[1,2,4]triazole 

Relevant articles and documents

Synthesis and structure-activity relationship of C-3 substituted triazolylthiomethyl cephems

A series of C-3 substituted triazolylthiomethyl cephems with an aminothiazolemethoxyiminoacetamido side chain at C-7 were synthesized and tested for antimicrobial activity against clinically-relevant isolates. The compound with 3-pyridyl at C-5 and methyl at N-4 of the triazole moiety exhibited good antibacterial activity against both Gram-positive and Gram-negative bacteria, with the exception of pseudomonas spp against which none of the derivatives exhibited favorable activity.

Recherches en serie triazepine XVI. Condensation des composes β-dicarbonyles avec les thiosemicarbazides

Condensations of β-dicarbonyl compounds with thiosemicarbazide and 1- and 2-methylthiosemicarbazide give three types of heterocyclic compounds.Depending upon the reagents and experimental conditions, triazepinones, triazepines, 1,2,4-triazolines or pyrazoles are formed.Mechanisms explaining these cyclisations are proposed.